About this trial
This study is a randomized, controlled trial with a pre-test/post-test design, conducted to determine the effects of Generative AI (GenAI)-supported learning on academic achievement, learning efficiency, and critical thinking within a university setting. The study population consists of students from the Dialysis Program at Bingöl University's Vocational School of Health Services; the sample comprises 100 volunteer students who met the inclusion criteria and were randomly assigned to either an experimental group (n=50) or a control group (n=50). The experimental group will participate in a "Generative AI-Supported Learning Program" over the course of one month-meeting two days a week for a total of eight 60-minute sessions-covering topics ranging from effective prompting techniques to case analysis and academic ethics; meanwhile, the control group will continue with their routine educational activities. Data will be collected using a Demographic Information Form, the Academic Achievement Inventory, the Critical Thinking Disposition Scale, and the Artificial Intelligence Dependency Scale, and will be analyzed using biostatistical methods (t-tests, ANCOVA, and effect size calculations).
Eligibility criteria
Qualifiers
Being an active undergraduate student enrolled in the university program/course during the study period
Willingness to voluntarily participate in the study and providing written informed consent
Having regular access to a digital device (e.g., smartphone, laptop, tablet) and an internet connection
Basic digital literacy to use educational software and AI tools
Disqualifiers
Prior formal or advanced training in generative AI tools (e.g., prompt engineering certification)
Transfer students or students repeating the course who have prior experience with the course material
Having cognitive, visual, or physical impairments that prevent participation in online learning or completing evaluation surveys
Unwillingness to participate in the study or withdrawing consent at any stage
Trial design
Treatments tested in this trial
- Behavioral